Sr. Biostatistician; Neurology

Sr. Biostatistician position with responsibilities across clinical trials and longitudinal studies in collaboration with investigators and a multidisciplinary team.

• Work with a multidisciplinary group on clinical trials and other longitudinal studies.
• Collaborate with investigators on research projects with primary responsibility for analysis and presentation of project data.
• Provide integration and analysis of biodata from multiple sources.
• Provide expertise in statistical design, data management, and data analysis.
• Contribute to the development and application of statistical methods to advance scientific goals of various projects.
• Serve as lead Biostatistician with investigators to develop objectives, design sampling, randomization, and statistical analysis plans to achieve study objectives.
• Design and perform appropriate methodologic procedures for statistical analysis, overall descriptive statistics, exploratory data analyses, including graphs, schematic summaries, and necessary transformations and confirmatory data analyses, including statistical tests and/or modeling.
• Design, implement, and manage computerized systems for analysis of complex research projects to prepare scientific presentations related to study results.
• Perform sample size and power calculations, generate randomization schema, and prepare statistical sections for research protocols and manuscripts.
• Participate in regularly scheduled meetings with investigators and team that require statistical input.
• Design tables and statistical procedures for specific research studies.
• Write statistical design, methods, and analysis for manuscripts and research proposals.
• Analyze data and prepare tables for interim and final reports.
• Develop and apply new statistical methodologies.
• Ensure data integrity and compliance with security policies governed by HIPAA and the Johns Hopkins IRB.
• Oversight of one or more professional team members and project milestones.
• Prepare progress reports and present to trial leadership.
• Oversee production of TLFs to support safety reviews (including DSMBs), publications, and ongoing study reporting.
• Program additional ad hoc requests to support clinical trial conduct and reporting including sample size calculations and data missingness.
• Identify data discrepancies and collaborate with trial leadership to resolve.
• Collaborate with project management to develop analytic timelines and deliverables.
• Lead development of specifications for derived datasets used to generate data summaries and statistical analysis.
• Other duties as assigned.

• Master s Degree in Biostatistics, Epidemiology, or related quantitative field.
• Three years related experience.
• Additional education may substitute for required experience, and additional related experience may substitute for required education beyond a high school diploma/graduation equivalent, to the extent permitted by the JHU equivalency formula.